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Spinocerebellar Ataxia type 17 presenting with progressive myoclonic epilepsy

• SCA17 should be included in the differential diagnoses of PMEs. • SCA17 is characterized by cerebellar features, myoclonic epilepsy, cognitive decline, psychiatric features, and chorea. • Subtle clinical signs like chorea can provide additional diagnostic clues to SCA17(HDL4), a Huntington disease...

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Detalles Bibliográficos
Autores principales:	Boongird, Apisit, Termsarasab, Pichet, Pulkes, Teeratorn
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2023
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160684/ https://www.ncbi.nlm.nih.gov/pubmed/37152277 http://dx.doi.org/10.1016/j.ensci.2023.100463

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